Fujita T, Fujimoto Y
Jpn J Pharmacol. 1981 Oct;31(5):795-800. doi: 10.1254/jjp.31.795.
Effect of various diuretics of lipid peroxidation in rat kidney cortical mitochondria and in the supernatant (11,000 x g) was studied. Mersalyl (mercurial diuretic) markedly stimulated the lipid peroxidation in mitochondria and in the supernatant at a concentration of 1 mM, and metolazone (sulfonamide derivative, 1 mM) stimulated only that in the supernatant. Mersalyl-induced lipid peroxidation was markedly inhibited by several classical radical scavengers such as sodium diethyldithiocarbamate, 2,6-di-tert-butylphenol and N,N'-diphenyl-p-phenylenediamine, but metolazone-induced lipid peroxidation was not inhibited by these scavengers. The addition of superoxide dismutase to the reaction mixture inhibited the mersalyl-induced lipid peroxidation, but did not inhibit the peroxidation by metolazone or ascorbate. These results suggest that lipid peroxidation by mersalyl is mediated by free radicals or superoxide anion, which were probably produced by mersalyl, and the mercurial diuretics-induced nephrotoxicity may be due to the lipid peroxidation in the kidney.
研究了各种利尿剂对大鼠肾皮质线粒体和上清液(11,000×g)中脂质过氧化的影响。汞撒利(汞利尿剂)在1 mM浓度时显著刺激线粒体和上清液中的脂质过氧化,而美托拉宗(磺胺衍生物,1 mM)仅刺激上清液中的脂质过氧化。汞撒利诱导的脂质过氧化被几种经典的自由基清除剂如二乙基二硫代氨基甲酸钠、2,6-二叔丁基苯酚和N,N'-二苯基对苯二胺显著抑制,但美托拉宗诱导的脂质过氧化不被这些清除剂抑制。向反应混合物中添加超氧化物歧化酶抑制了汞撒利诱导的脂质过氧化,但不抑制美托拉宗或抗坏血酸诱导的过氧化。这些结果表明,汞撒利引起的脂质过氧化是由自由基或超氧阴离子介导的,它们可能是由汞撒利产生的,汞利尿剂诱导的肾毒性可能归因于肾脏中的脂质过氧化。